PROVENT NASAL CANNULA — Ventus Medical, Inc. (510(k) K080983)
PROVENT NASAL CANNULA — Ventus Medical, Inc. (510(k) K080983) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: PROVENT NASAL CANNULA; Applicant: Ventus Medical, Inc.; Clearance track: 510(k).
| Device name | PROVENT NASAL CANNULA |
|---|---|
| Applicant | Ventus Medical, Inc. |
| Clearance track | 510(k) |
| Submission number | K080983 |
| Decision | Substantially Equivalent |
| Decision date | 2008-08-07 |
| Date received | 2008-04-07 |
| Product code | MNR |
| Device class | 2 |
| Medical specialty | Anesthesiology |
| Applicant location | CA, US |
| Source | openFDA device |
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$1999/mo
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